The drosophila zinc finger protein trade embargo is required for double strand break formation in meiosis

PLoS Genetics

Volumn 7, Issue 2, 2011, Pages

  Lake, Cathleen M ^a   Nielsen, Rachel J ^a   Hawley, R Scott ^a,b  

^a STOWERS INSTITUTE FOR MEDICAL RESEARCH   (United States)

^b UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; PROTEIN MEI P22; TRADE EMBARGO PROTEIN; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN; DROSOPHILA PROTEIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CHROMATIN STRUCTURE; CHROMOSOME; CONTROLLED STUDY; DNA REPAIR; DOUBLE STRANDED DNA BREAK; DROSOPHILA; FEMALE; GENETIC RECOMBINATION; MALE; MEIOSIS; NONHUMAN; OOCYTE; OOCYTE DEVELOPMENT; PROTEIN ANALYSIS; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; CYTOLOGY; DROSOPHILA MELANOGASTER; GENETICS; METABOLISM; MOLECULAR GENETICS; MUTATION; SEQUENCE ALIGNMENT;

AMINO ACID SEQUENCE; ANIMALS; DNA BREAKS, DOUBLE-STRANDED; DNA REPAIR; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; FEMALE; MEIOSIS; MOLECULAR SEQUENCE DATA; MUTATION; OOCYTES; SEQUENCE ALIGNMENT; ZINC FINGERS;

EID: 79952256612     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1002005     Document Type: Article

References (51)

1. Murakami H, Keeney S, (2008) Regulating the formation of DNA double-strand breaks in meiosis. Genes & Development 22: 286-292.
2. Keeney S, (2001) Mechanism and control of meiotic recombination initiation. Current Topics in Developmental Biology: Academic Press pp. 1-53.
3. Bergerat A, de Massy B, Gadelle D, Varoutas P-C, Nicolas A, et al. (1997) An atypical topoisomerase II from archaea with implications for meiotic recombination. Nature 386: 414-417.
4. Keeney S, Giroux CN, Kleckner N, (1997) Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family. Cell 88: 375-384.
5. McKim KS, Hayashi-Hagihara A, (1998) mei-W68 in Drosophila melanogaster encodes a Spo11 homolog: evidence that the mechanism for initiating meiotic recombination is conserved. Genes Dev 12: 2932-2942.
6. Jang JK, Sherizen DE, Bhagat R, Manheim EA, McKim KS, (2003) Relationship of DNA double-strand breaks to synapsis in Drosophila. J Cell Sci 116: 3069-3077.
7. Liu H, Jang JK, Kato N, McKim KS, (2002) mei-P22 Encodes a Chromosome-Associated Protein Required for the Initiation of Meiotic Recombination in Drosophila melanogaster. Genetics 162: 245-258.
8. Mehrotra S, McKim KS, (2006) Temporal Analysis of Meiotic DNA Double-Strand Break Formation and Repair in Drosophila Females. PLoS Genet 2: e200 doi:10.1371/journal.pgen.0020200.
9. McKim KS, Jang JK, Theurkauf WE, Hawley RS, (1993) Mechanical basis of meiotic metaphase arrest. Nature 362: 364-366.
10. Jang JK, Messina L, Erdman MB, Arbel T, Hawley RS, (1995) Induction of metaphase arrest in Drosophila oocytes by chiasma-based kinetochore tension. Science 268: 1917-1919.
11. Baker BS, Hall JC, (1976) Meiotic mutants: genetic control of meiotic recombination and chromosome segregation. In: Ashburner M, Novitski E, editors. The Genetics and Biology of Drosophila Vol 1a New York, NY Academic Press pp. 351-434.
12. Hawley RS, McKim KS, Arbel T, (1993) Meiotic segregation in Drosophila melanogaster females: molecules, mechanisms, and myths. Annu Rev Genet pp. 281-317.
13. Page SL, Nielsen R, Teeter K, Lake CM, Ong S, et al. (2007) A Germline Clone Screen for Meiotic Mutants in Drosophila melanogaster. FLY 1: 172-181.
14. Thibault ST, Singer MA, Miyazaki WY, Milash B, Dompe NA, et al. (2004) A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac. Nat Genet 36: 283-287.
15. Rorth P, (1998) Gal4 in the Drosophila female germline. Mech Dev 78: 113-118.
16. Koundakjian EJ, Cowan DM, Hardy RW, Becker AH, (2004) The Zuker Collection: A Resource for the Analysis of Autosomal Gene Function in Drosophila melanogaster. Genetics 167: 203-206.
17. Brayer K, Kulshreshtha S, Segal D, (2008) The Protein-Binding Potential of C2H2 Zinc Finger Domains. Cell Biochemistry and Biophysics 51: 9-19.
18. Chung H-R, Schäfer U, Herbert J, Böhm S, (2002) Genomic expansion and clustering of ZAD-containing C2H2 zinc-finger genes in Drosophila. EMBO reports 3: 1158-1162.
19. Chung H-R, Lohr U, Jackle H, (2007) Lineage-specific expansion of the Zinc Finger Associated Domain ZAD. Molecular Biology and Evolution 24: 1934-1943.
20. Payre F, Buono P, Vanzo N, Vincent A, (1997) Two types of zinc fingers are required for dimerization of the serendipity delta transcriptional activator. Mol Cell Biol 17: 3137-3145.
21. Jauch R, Bourenkov GP, Chung H-R, Urlaub H, Reidt U, et al. (2003) The Zinc Finger-Associated Domain of the Drosophila Transcription Factor Grauzone Is a Novel Zinc-Coordinating Protein-Protein Interaction Module. Structure (London, England: 1993) 11: 1393-1402.
22. Ghabrial A, Ray RP, Schupbach T, (1998) okra and spindle-B encode components of the RAD52 DNA repair pathway and affect meiosis and patterning in Drosophila oogenesis. Genes & Development 12: 2711-2723.
23. Pabo CO, Peisach E, Grant RA, (2001) Design and selection of novel Cys2His2 zinc finger proteins. Annual Review of Biochemistry 70: 313-340.
24. Gilliland WD, Hughes SF, Vietti DR, Hawley RS, (2009) Congression of achiasmate chromosomes to the metaphase plate in Drosophila melanogaster oocytes. Dev Biol 325: 122-128.
25. Ghabrial A, Schupbach T, (1999) Activation of a meiotic checkpoint regulates translation of Gurken during Drosophila oogenesis. Nat Cell Biol 1: 354-357.
26. Iuchi S, (2001) Three classes of C2H2 zinc finger proteins. Cellular and Molecular Life Sciences 58: 625-635.
27. Baudat F, Buard J, Grey C, Fledel-Alon A, Ober C, et al. (2010) PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice. Science 327: 836-840.
28. Myers S, Bowden R, Tumian A, Bontrop RE, Freeman C, et al. (2010) Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination. Science 327: 876-879.
29. Parvanov ED, Petkov PM, Paigen K, (2010) Prdm9 Controls Activation of Mammalian Recombination Hotspots. Science 327: 835.
30. Myers S, Freeman C, Auton A, Donnelly P, McVean G, (2008) A common sequence motif associated with recombination hot spots and genome instability in humans. Nat Genet 40: 1124-1129.
31. Buard J, Barthes P, Grey C, de Massy B, (2009) Distinct histone modifications define initiation and repair of meiotic recombination in the mouse. EMBO J 28: 2616-2624.
32. Borde V, Robine N, Lin W, Bonfils S, Geli V, et al. (2009) Histone H3 lysine 4 trimethylation marks meiotic recombination initiation sites. EMBO J 28: 99-111.
33. Berg IL, Neumann R, Lam K-WG, Sarbajna S, Odenthal-Hesse L, et al. (2010) PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans. Nat Genet 42: 859-863.
34. Martini E, Diaz RL, Hunter N, Keeney S, (2006) Crossover Homeostasis in Yeast Meiosis. Cell 126: 285-295.
35. McKim KS, Green-Marroquin BL, Sekelsky JJ, Chin G, Steinberg C, et al. (1998) Meiotic synapsis in the absence of recombination. Science 279: 876-878.
36. Joyce EF, McKim KS, (2009) Drosophila PCH2 Is Required for a Pachytene Checkpoint That Monitors Double-Strand-Break-Independent Events Leading to Meiotic Crossover Formation. Genetics 181: 39-51.
37. Baker BS, Hall JC, (1976) Meiotic Mutants: Genetic control of of meiotic recombination and chromosome segregation. In: Ashburner M, Novitski E, editors. The Genetics and Biology of Drosophila London Academic Press pp. 352-434.
38. Carpenter AT, Sandler L, (1974) On recombination-defective meiotic mutants in Drosophila melanogaster. Genetics 76: 453-475.
39. Bhagat R, Manheim EA, Sherizen DE, McKim KS, (2004) Studies on crossover-specific mutants and the distribution of crossing over in Drosophila females. Cytogenetic and Genome Research 107: 160-171.
40. Markstein M, Pitsouli C, Villalta C, Celniker SE, Perrimon N, (2008) Exploiting position effects and the gypsy retrovirus insulator to engineer precisely expressed transgenes. Nat Genet 40: 476-483.
41. Zimmering S, (1976) Genetic and cytogenetic aspects of altered segregation phenomena in Drosophila. In: Ashburner M, Novitski E, editors. The Genetics and Biology of Drosophila Vol 1a New York Academic Press pp. 569-613.
42. Matsubayashi H, Yamamoto M-T, (2003) REC, a new member of the MCM-related protein family, is required for meiotic recombination in Drosophila. Genes & Genetic Systems 78: 363-371.
43. Page SL, McKim KS, Deneen B, Van Hook TL, Hawley RS, (2000) Genetic studies of mei-P26 reveal a link between the processes that control germ cell proliferation in both sexes and those that control meiotic exchange in Drosophila. Genetics 155: 1757-1772.
44. Page SL, Hawley RS, (2001) c(3)G encodes a Drosophila synaptonemal complex protein. Genes Dev 15: 3130-3143.
45. Gloor GB, Preston CR, Johnson-Schlitz DM, Nassif NA, Phillis RW, et al. (1993) Type I Repressors of P Element Mobility. Genetics 135: 81-95.
46. Matthies HJ, Messina L, Namba R, Greer KJ, Walker MY, et al. (2000) Analysis of Meiosis in Fixed and Live Oocytes by Light Microscopy. In: Sullivan WS, Ashburner M, Hawley RS, editors. Drosophila: Protocols New York Cold Spring Harbor Press pp. 67-85.
47. Lantz V, Chang JS, Horabin JI, Bopp D, Schedl P, (1994) The Drosophila orb RNA-binding protein is required for the formation of the egg chamber and establishment of polarity. Genes & Development 8: 598-613.
48. Anderson LK, Royer SM, Page SL, McKim KS, Lai A, et al. (2005) Juxtaposition of C(2)M and the transverse filament protein C(3)G within the central region of Drosophila synaptonemal complex. Proc Natl Acad Sci U S A 102: 4482-4487.
49. Liang L, Diehl-Jones W, Lasko P, (1994) Localization of vasa protein to the Drosophila pole plasm is independent of its RNA-binding and helicase activities. Development 120: 1201-1211.
50. King RC, Rubinson AC, Smith RF, (1956) Oogenesis in adult Drosophila melanogaster. Growth 20: 121-157.
51. Page SL, Khetani RS, Lake CM, Nielsen RJ, Jeffress JK, et al. (2008) Corona is required for higher-order assembly of transverse filaments into full-length synaptonemal complex in Drosophila oocytes. PLoS Genet 4: e1000194 doi:10.1371/journal.pgen.1000194.